Taiwan FDA registration d8a69f00fa6a083139133b3e4c03032f

"Rivanova" Yili Flow double catheter

TW: “里凡諾瓦”宜立流雙導管

Taiwan·Risk Class 2·LivaNova USA, Inc.·Registered May 28, 2015 – May 28, 2030Active

Registration details

Analysis ID: d8a69f00fa6a083139133b3e4c03032f
Customs Code: DHA05602730904

Company information

Manufacturer: LivaNova USA, Inc.
Manufacturer Country: United States
Authorized Representative: INTERLINK MEDICAL ENTERPRISE CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
Import Information: import

Dates and status

Registration Date: May 28, 2015
Expiry Date: May 28, 2030

About this record

Access comprehensive regulatory information for "Rivanova" Yili Flow double catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d8a69f00fa6a083139133b3e4c03032f and manufactured by LivaNova USA, Inc.. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.